Actively Recruiting
Ejaculatory and Orgasmic Dysfunction Registry
Led by Charitable Union for the Research and Education of Peyronie's Disease · Updated on 2025-02-14
500
Participants Needed
1
Research Sites
261 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to evaluate the safety and efficacy of various therapies used to treat ejaculatory and/or orgasmic dysfunctions in men. The objective is to create a large, national registry designed to capture key outcomes for men being treated for ejaculatory and/or orgasmic dysfunction. Participants will submit questionnaires about their diagnosis and treatment efficacy and multiple time intervals.
CONDITIONS
Official Title
Ejaculatory and Orgasmic Dysfunction Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men being treated for either ejaculatory and/or orgasmic dysfunction
- Being a sexual partner of a man with ejaculatory and/or orgasmic dysfunction who is receiving treatment
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Male Fertility and Peyronie's Clinic
Orem, Utah, United States, 84057
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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